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The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission
Genes and neural circuits coordinately regulate animal sleep. However, it remains elusive how these endogenous factors shape sleep upon environmental changes. Here, we demonstrate that Shaker (Sh)-expressing GABAergic neurons projecting onto dorsal fan-shaped body (dFSB) regulate temperature-adaptiv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160125/ https://www.ncbi.nlm.nih.gov/pubmed/32296133 http://dx.doi.org/10.1038/s42003-020-0902-8 |
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author | Kim, Ji-hyung Ki, Yoonhee Lee, Hoyeon Hur, Moon Seong Baik, Bukyung Hur, Jin-Hoe Nam, Dougu Lim, Chunghun |
author_facet | Kim, Ji-hyung Ki, Yoonhee Lee, Hoyeon Hur, Moon Seong Baik, Bukyung Hur, Jin-Hoe Nam, Dougu Lim, Chunghun |
author_sort | Kim, Ji-hyung |
collection | PubMed |
description | Genes and neural circuits coordinately regulate animal sleep. However, it remains elusive how these endogenous factors shape sleep upon environmental changes. Here, we demonstrate that Shaker (Sh)-expressing GABAergic neurons projecting onto dorsal fan-shaped body (dFSB) regulate temperature-adaptive sleep behaviors in Drosophila. Loss of Sh function suppressed sleep at low temperature whereas light and high temperature cooperatively gated Sh effects on sleep. Sh depletion in GABAergic neurons partially phenocopied Sh mutants. Furthermore, the ionotropic GABA receptor, Resistant to dieldrin (Rdl), in dFSB neurons acted downstream of Sh and antagonized its sleep-promoting effects. In fact, Rdl inhibited the intracellular cAMP signaling of constitutively active dopaminergic synapses onto dFSB at low temperature. High temperature silenced GABAergic synapses onto dFSB, thereby potentiating the wake-promoting dopamine transmission. We propose that temperature-dependent switching between these two synaptic transmission modalities may adaptively tune the neural property of dFSB neurons to temperature shifts and reorganize sleep architecture for animal fitness. |
format | Online Article Text |
id | pubmed-7160125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71601252020-04-24 The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission Kim, Ji-hyung Ki, Yoonhee Lee, Hoyeon Hur, Moon Seong Baik, Bukyung Hur, Jin-Hoe Nam, Dougu Lim, Chunghun Commun Biol Article Genes and neural circuits coordinately regulate animal sleep. However, it remains elusive how these endogenous factors shape sleep upon environmental changes. Here, we demonstrate that Shaker (Sh)-expressing GABAergic neurons projecting onto dorsal fan-shaped body (dFSB) regulate temperature-adaptive sleep behaviors in Drosophila. Loss of Sh function suppressed sleep at low temperature whereas light and high temperature cooperatively gated Sh effects on sleep. Sh depletion in GABAergic neurons partially phenocopied Sh mutants. Furthermore, the ionotropic GABA receptor, Resistant to dieldrin (Rdl), in dFSB neurons acted downstream of Sh and antagonized its sleep-promoting effects. In fact, Rdl inhibited the intracellular cAMP signaling of constitutively active dopaminergic synapses onto dFSB at low temperature. High temperature silenced GABAergic synapses onto dFSB, thereby potentiating the wake-promoting dopamine transmission. We propose that temperature-dependent switching between these two synaptic transmission modalities may adaptively tune the neural property of dFSB neurons to temperature shifts and reorganize sleep architecture for animal fitness. Nature Publishing Group UK 2020-04-15 /pmc/articles/PMC7160125/ /pubmed/32296133 http://dx.doi.org/10.1038/s42003-020-0902-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Ji-hyung Ki, Yoonhee Lee, Hoyeon Hur, Moon Seong Baik, Bukyung Hur, Jin-Hoe Nam, Dougu Lim, Chunghun The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title | The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title_full | The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title_fullStr | The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title_full_unstemmed | The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title_short | The voltage-gated potassium channel Shaker promotes sleep via thermosensitive GABA transmission |
title_sort | voltage-gated potassium channel shaker promotes sleep via thermosensitive gaba transmission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160125/ https://www.ncbi.nlm.nih.gov/pubmed/32296133 http://dx.doi.org/10.1038/s42003-020-0902-8 |
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